Long-term effectiveness of ustekinumab comparable to antitumor necrosis factor agents in patients with Crohn's disease.
Crohn's disease
adalimumab
anti-tumor necrosis factor
infliximab
ustekinumab
Journal
Journal of gastroenterology and hepatology
ISSN: 1440-1746
Titre abrégé: J Gastroenterol Hepatol
Pays: Australia
ID NLM: 8607909
Informations de publication
Date de publication:
Nov 2022
Nov 2022
Historique:
revised:
10
08
2022
received:
09
06
2022
accepted:
30
08
2022
pubmed:
6
9
2022
medline:
22
11
2022
entrez:
5
9
2022
Statut:
ppublish
Résumé
Ustekinumab (UST), an antibody against the p40 subunit of interleukin-12/23, has been proven to be effective in patients with Crohn's disease (CD). However, large, long-term comparative studies of UST against anti--tumor necrosis factor (TNF) agents are lacking. We compared the effectiveness of anti-TNF agents and UST in CD patients without prior use of biologics. We used a large nationwide anonymized Japanese database containing administrative medical claims data and various related patient data. In a propensity score-matched cohort with similar clinical characteristics, 2-year effectiveness was compared between patients treated with infliximab or adalimumab (anti-TNF group) and those treated with UST (UST group). Primary outcomes were cumulative rates of hospitalization, surgery, and persistence. Among 53 540 CD patients, 7047 were extracted for eligibility, of which 5665 were treated with an anti-TNF agent and 1382 with UST. After propensity score matching, the cumulative hospitalization rates were comparable between anti-TNF and UST groups (P = 0.85; 25.3% vs 26.5% at 1 year, 33.8% vs 39.8% at 2 years). The cumulative surgery rates were also comparable between these groups (P = 0.46; 5.5% vs 5.1% at 1 year, 8.3% vs 8.4% at 2 years). The persistence rate at 1 year was higher in UST group (90.8% vs 92.5%), and that at 2 years was higher in anti-TNF group (81.2% and 74.6%); however, there was no significant difference in the cumulative persistence rate (P = 0.55). Anti-TNF agents and UST appear to have comparable effectiveness for CD patients without prior use of biologics.
Sections du résumé
BACKGROUND
BACKGROUND
Ustekinumab (UST), an antibody against the p40 subunit of interleukin-12/23, has been proven to be effective in patients with Crohn's disease (CD). However, large, long-term comparative studies of UST against anti--tumor necrosis factor (TNF) agents are lacking. We compared the effectiveness of anti-TNF agents and UST in CD patients without prior use of biologics.
METHODS
METHODS
We used a large nationwide anonymized Japanese database containing administrative medical claims data and various related patient data. In a propensity score-matched cohort with similar clinical characteristics, 2-year effectiveness was compared between patients treated with infliximab or adalimumab (anti-TNF group) and those treated with UST (UST group). Primary outcomes were cumulative rates of hospitalization, surgery, and persistence.
RESULTS
RESULTS
Among 53 540 CD patients, 7047 were extracted for eligibility, of which 5665 were treated with an anti-TNF agent and 1382 with UST. After propensity score matching, the cumulative hospitalization rates were comparable between anti-TNF and UST groups (P = 0.85; 25.3% vs 26.5% at 1 year, 33.8% vs 39.8% at 2 years). The cumulative surgery rates were also comparable between these groups (P = 0.46; 5.5% vs 5.1% at 1 year, 8.3% vs 8.4% at 2 years). The persistence rate at 1 year was higher in UST group (90.8% vs 92.5%), and that at 2 years was higher in anti-TNF group (81.2% and 74.6%); however, there was no significant difference in the cumulative persistence rate (P = 0.55).
CONCLUSIONS
CONCLUSIONS
Anti-TNF agents and UST appear to have comparable effectiveness for CD patients without prior use of biologics.
Identifiants
pubmed: 36059265
doi: 10.1111/jgh.15992
pmc: PMC9826487
doi:
Substances chimiques
Ustekinumab
FU77B4U5Z0
Tumor Necrosis Factor Inhibitors
0
Infliximab
B72HH48FLU
Adalimumab
FYS6T7F842
Tumor Necrosis Factor-alpha
0
Biological Products
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
2105-2112Informations de copyright
© 2022 The Authors. Journal of Gastroenterology and Hepatology published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd.
Références
J Gastroenterol Hepatol. 2020 Feb;35(2):225-232
pubmed: 31397010
Clin Gastroenterol Hepatol. 2022 Mar;20(3):578-590.e4
pubmed: 33618023
J Gastroenterol Hepatol. 2022 Nov;37(11):2105-2112
pubmed: 36059265
Clin Gastroenterol Hepatol. 2022 Jul;20(7):1579-1587.e2
pubmed: 33838348
J Crohns Colitis. 2021 Mar 5;15(3):358-366
pubmed: 32845311
Aliment Pharmacol Ther. 2019 Aug;50(3):278-288
pubmed: 31222872
Aliment Pharmacol Ther. 2020 Jul;52(1):123-134
pubmed: 32441396
Aliment Pharmacol Ther. 2020 May;51(10):948-957
pubmed: 32249966
Clin Gastroenterol Hepatol. 2021 Apr;19(4):668-679.e8
pubmed: 32629124
N Engl J Med. 2016 Nov 17;375(20):1946-1960
pubmed: 27959607
Lancet. 2022 Jun 11;399(10342):2200-2211
pubmed: 35691323
J Crohns Colitis. 2020 Jan 1;14(1):33-45
pubmed: 31219157
Aliment Pharmacol Ther. 2020 Oct;52(8):1341-1352
pubmed: 32955122
J Crohns Colitis. 2019 Oct 28;13(11):1401-1409
pubmed: 30989232
Clin Gastroenterol Hepatol. 2019 Jul;17(8):1525-1532.e1
pubmed: 30267864
J Epidemiol. 2017 Oct;27(10):476-482
pubmed: 28142051
Lancet Gastroenterol Hepatol. 2021 Dec;6(12):1002-1014
pubmed: 34688373
J Crohns Colitis. 2021 Nov 8;15(11):1920-1930
pubmed: 33909062
Clin Gastroenterol Hepatol. 2021 Oct;19(10):2082-2092.e10
pubmed: 32801006
J Crohns Colitis. 2020 Jan 1;14(1):4-22
pubmed: 31711158
J Gastroenterol Hepatol. 2021 Jun;36(6):1598-1604
pubmed: 33119929
Aliment Pharmacol Ther. 2020 Sep;52(6):1017-1030
pubmed: 32770851
Clin Gastroenterol Hepatol. 2021 Jul;19(7):1366-1376.e2
pubmed: 32668338
Aliment Pharmacol Ther. 2018 Aug;48(4):394-409
pubmed: 29920733